http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2068807-T3

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filingDate 1987-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1995-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ea73445118c3ce762cae237cc11fa24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db011002def30cd5b6ece4dd45aeeb04
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publicationDate 1995-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2068807-T3
titleOfInvention CARBOESTIRILE DERIVATIVES, PROCEDURE TO PREPARE THEM, PHARMACEUTICAL COMPOSITION, AND USE.
abstract The use of a carbostyril derivative or a salt thereof represented by the general formula (1), ** formula ** where R is an unsaturated heterocyclic residual group selected from the groups 1,2,4 -triazolyl, imidazolyl, 1, 2,3,5-tetrazolyl, 1,2,3,4-tetrazolyl, pyrrolyl, benzimidazolyl, 1,3,4 -triazolyl, imidazolinyl, pyridyl, pyrimidinyl, pyrazolyl, pyrazolinyl, thiazolyl, thiazolinyl, 1,3,4 - oxadiazolyl, 1,3,4-thiadiazolyl, thienyl, furyl, pyranyl, isothiazolyl, isoxazolyl, pyrazinyl, pyridazinyl, indolyl, isoindolyl, 3H-indolyl, indolizinyl, indazolyl, quinolyl, isoquinolinylyl, chinolidinyl, chinylidinyl, choline, naphthyridinyl, chinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl, zinyl. pyrrolinyl, pyrazolinyl, indolinyl and isoindolinyl, said unsaturated heterocyclic residual group can have from 1 to 3 substituents, heterocyclic residual over ring, selected from an oxo group; an uncle group; a group-phenyl; a group-phenyl that may have from 1 to 3 substituents, a defenyl ring, selected from a C1-C6 alkyl group, a C1-C6 haloalkyl group, a halogen atom, a hydroxy group, an amino group, an amino (C1-C6) alkyl group, a carboxy group and a C1-C6 alkoxy group; a C3-C8 cycloalkyl group; a phenylthio group; a C1-C6 alkyl group; a C1-C6 alkyl group having 1 to 2 substituents selected from an amino group, a (C1-C6) alkyl amino group and a carboxyl group; an amino group; a hydroxyl group; a cyano group; a carboxyl group; a (C1-C6) alkoxycarbonyl group; a C1-C6 phenylalkyl group which may have hydroxyl groups as substituents on the phenyl ring; a phenylsulfonyl group which may have C1-C6 alkyl groups as substituents on the phenyl ring; a C1-C6 phenylalkyl substituted with C1-C6 alkoxy; a (C1-C6) alkyl thio group; a C2-C6 alkenyl group; a C1-C6 alkoxy group and a pyridyl group; R1 is a hydrogen atom, a C1-C6 alkyl group, or a C1-C6 phenylalkyl group; R2 is a hydrogen atom, a halogen atom, a (C1-C6) alkyl sulfonyloxy group, a C1-C6 alkoxy group, or a hydroxyl group; Z is an oxygen atom, a sulfur atom, a group of the formula -C - !! Or, a group of formula -C - !! N -OH a group of formula -CH - !! OR3 (where R3 is a hydrogen atom or a C1-C6 alkyl group) or a group of the formula -NH-; A is a C2-C6 alkylene group; X is an oxygen atom, a sulfur atom, a group of the formula - SO - or a group of the formula - SO2 -; n is 0 or 1; and the carbon-carbon bond between positions 3 and 4 of the carbostyril skeleton is a single or double bond in the preparation of a drug for the treatment and prevention of arteriosclerosis, ischemic heart disease, chronic arterial obstruction, nephritis acute or chronic and treatment during artificial dialysis and implantation of an artificial organ.
priorityDate 1986-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 45.